Label: MOSCO- salicylic acid plaster

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 13, 2017

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Salicylic Acid 40%

  • Purpose

    Corn remover

  • Use

    For the removal of corns

  • Warnings

    For external use only

    Do not use

    • on irritated skin
    • on any area that is infected or reddened
    • if you have diabetes or poor blood circulation

    Stop use and ask a doctor

    if discomfort persists

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • wash affected area
    • may soak corn in warm water for 5 minutes
    • dry thoroughly
    • remove medicated pad from backing paper by pulling from center of pad
    • apply
    • repeat procedure every 48 hours as needed for up to 14 days (until corn is removed)
  • Other information

    • store at room temperature
    • avoid excessive heat
  • Inactive ingredients

    lanolin, polybutene, rosin ester, rubber

  • Questions?

    1-800-443-4908

  • PRINCIPAL DISPLAY PANEL

    MOSCO Maximum Strength One Step Corn Remover Pads

    Salicylic Acid 40%

    8 Pads

    MOSCO One Step Corn Remover Pads Carton

  • INGREDIENTS AND APPEARANCE
    MOSCO 
    salicylic acid plaster
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-310
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID4 mg
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN (UNII: 7EV65EAW6H)  
    POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)  
    NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63029-310-088 in 1 CARTON; Type 0: Not a Combination Product01/08/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358F01/08/2010
    Labeler - Medtech Products Inc. (122715688)
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